CV Therapeutics Reports 2006 Third Quarter Financial Results
Tuesday October 31, 4:01 pm ET
PALO ALTO, Calif., Oct. 31 /PRNewswire-FirstCall/ -- CV Therapeutics, Inc. (Nasdaq: CVTX - News) today reported financial results for the three and nine months ended September 30, 2006.
ADVERTISEMENT
For the quarter ended September 30, 2006, the Company reported a net loss of $62.7 million, or $1.23 per share. This compares to a net loss of $55.9 million, or $1.26 per share, for the same quarter in 2005 and to a net loss of $73.1 million or $1.59 per share, for the prior quarter ended June 30, 2006. For the nine months ended September 30, 2006, the Company reported a net loss of $206.3 million, or $4.36 per share, compared to a net loss of $153.9 million, or $3.98 per share, for the nine months ended September 30, 2005. At September 30, 2006, the Company had cash, cash equivalents, marketable securities and restricted cash of approximately $373.3 million, compared to $481.8 million at December 31, 2005.
For the quarter ended September 30, 2006, the Company recorded $8.2 million of net product revenue for sales of Ranexa® (ranolazine extended- release tablets), compared to net product revenue of $1.2 million for the prior quarter ended June 30, 2006. The $8.2 million of Ranexa product revenue recorded in the quarter ended September 30, 2006 included approximately $5.0 million related to product sales made in the quarter ended March 31, 2006, which was deferred due to product return privileges that expired in the quarter ended September 30, 2006. The Company received FDA approval for Ranexa on January 27, 2006 and commenced commercial product sales of Ranexa in March 2006.
The Company also recognized collaborative research revenue of $4.0 million for the quarter ended September 30, 2006. Collaborative research revenue recognized primarily relates to the reimbursement of certain regadenoson development costs from a collaborative partner and amortization of up-front payments earned. There was no co-promotion revenue recognized for the quarter ended September 30, 2006 related to sales of ACEON® (perindopril erbumine) Tablets since ACEON® product revenues in the quarter did not exceed the baseline specified in the amended co-promotion agreement with Solvay Pharmaceuticals, Inc.
Total costs and expenses were $76.3 million for the quarter ended September 30, 2006. This compares to total costs and expenses of $59.4 million for the same quarter in 2005 and $80.4 million for the prior quarter ended June 30, 2006. For the nine months ended September 30, 2006, total costs and expenses were $233.0 million compared to $167.6 million for the same period in the prior year.
The increase in total costs and expenses for the quarter ended September 30, 2006 compared to the same period in the prior year was primarily due to higher selling, general and administrative expenses associated with the Company's marketing of Ranexa, greater expenses associated with the Company's national cardiovascular specialty sales force (which was still being recruited in 2005), higher outside clinical trial expenses related to Phase 3 Ranexa development and other research programs and higher personnel related expenses including stock-based compensation in various functional areas to support the Company's increased commercialization and business activities. These increases were partially offset by lower marketing expenses related to the co-promotion of ACEON®.
The decrease in total costs and expenses for the quarter ended September 30, 2006 compared to the prior quarter ended June 30, 2006 was primarily due to lower marketing expenses related to the co-promotion of ACEON®, lower external general and administrative expenses and lower outside contract services expense for research and development activities related primarily to Ranexa and regadenoson.
The increase in total costs and expenses for the nine months ended September 30, 2006 compared to the same period in the prior year was primarily due to higher selling, general and administrative expenses associated with promotion activities related to Ranexa and the Company's national cardiovascular specialty sales force (which was still being recruited in 2005), higher expenses incurred to market Ranexa and higher personnel related expenses, including stock-based compensation, in various functional areas to support the Company's increased commercialization and business activities. These increases were partially offset by lower outside contract expenses for Phase 3 regadenoson development and lower marketing expenses related to the co-promotion of ACEON®.
The Company sent a notice of termination of the co-promotion agreement with Solvay Pharmaceuticals in October 2006 and has concluded its promotion of ACEON®. We do not anticipate booking any additional co-promotion revenue related to sales of ACEON®, and there are no future financial commitments for the Company related to the termination of the co-promotion agreement. Additionally, we do not expect the conclusion of the ACEON® co-promotion activities to have a material impact on the total sales and marketing expenses of the Company going forward.
Company management will webcast a conference call on October 31, 2006 at 5:00 p.m. EST, 2:00 p.m. PST, on the Company's website. To access the live webcast, please log on to the Company's website at www.cvt.com and go to the Investor Information section. Alternatively, domestic callers may participate in the conference call by dialing (888) 370-6121, and international callers may participate in the conference call by dialing (706) 679-7163. Webcast and telephone replays of the conference call will be available approximately two hours after the completion of the call through Tuesday, November 7, 2006. Domestic callers can access the replay by dialing (800) 642-1687, and international callers can access the replay by dialing (706) 645-9291; the PIN access number is 8804902.
About CV Therapeutics
CV Therapeutics, Inc., headquartered in Palo Alto, California, is a biopharmaceutical company focused on applying molecular cardiology to the discovery, development and commercialization of novel, small molecule drugs for the treatment of cardiovascular diseases.
CV Therapeutics' approved product, Ranexa® (ranolazine extended-release tablets), is indicated for the treatment of chronic angina in patients who have not achieved an adequate response with other antianginal drugs, and should be used in combination with amlodipine, beta-blockers or nitrates.
CV Therapeutics also has other clinical and preclinical drug development candidates and programs, including regadenoson, which is being developed for potential use as a pharmacologic stress agent in myocardial perfusion imaging studies and CVT-6883, which is being developed as a potential treatment for asthma and other conditions. Regadenoson and CVT-6883 have not been determined by any regulatory authorities to be safe or effective in humans for any use. |
